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Hypomethylation of the RUNX2 Gene Is a New Potential Biomarker of Primary Osteoporosis in Men and Women
Yalaev, Bulat, Tyurin, Anton, Akhiiarova, Karina, Khusainova, Rita (2024)
years of age of Russian ethnicity from the Volga-Ural region of Russia was carried out. The level of DNA
Central corneal thickness and its associations in a Russian population. The Ural eye and Medical Study
Bikbov, Mukharram M., Gilmanshin, Timur R., Zainullin, Rinat M., Kazakbaeva, Gyulli M., Zaynetdinov, Artur F., Nuriev, Ildar F., Panda-Jonas, Songhomitra, Arslangareeva, Inga I., Zinnatullin, Ainur A., Yakupova, Dilya F., Rakhimova, Ellina M., Uzianbaeva, Yulia V., Khikmatullin, Renat I., Nikitin, Nikolay A., Aminev, Said K., Mukhamadieva, Svetlana R., Mavlieva, Venera F., Jonas, Jost B. (2023)
.001), Russian ethnicity (beta:0.04; B:3.48; 95%CI:1.04, 5.91; P = 0.005), higher level of education (beta:0
КЛИНИЧЕСКИЙ И МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ АНАЛИЗ СЛУЧАЯ СЕМЕЙНОГО РАССЕЯННОГО СКЛЕРОЗА В РЕСПУБЛИКЕ БАШКОРТОСТАН
CLINICAL AND MOLECULAR GENETIC ANALYSIS OF A CASE OF FAMILIAL MULTIPLE SCLEROSIS IN THE REPUBLIC OF BASHKORTOSTAN
Заплахова, О.В., Тимашева, Я.Р., Бахтиярова, К.З., Туктарова, И.А., Мустафина, О.Е., Zaplakhova, O.V., Timasheva, Y.R., Bakhtiyarova, K.Z., Tuktarova, I.A., Mustafina, O.E. (2019)
of six affected members of one family. Material and methods. Six members of the family of Russian ethnic
СИНДРОМ МЮНХМЕЙЕРА: ГЕНЕТИЧЕСКИЕ МЕХАНИЗМЫ, ТЕХНОЛОГИИ ДИАГНОСТИКИ И ЛЕЧЕНИЯ
MUNCHMEYER SYNDROME: GENETIC MECHANISMS, DIAGNOSTIC AND TREATMENT TECHNOLOGIES
Батыршин, А. А., Batyrshin, A.A. (2024)
Анализ ассоциаций маркеров генетической предрасположенности, выявленных в полногеномных исследованиях с рассеянным склерозом
Analysis of Associations of Genetic Predisposition Markers Identified in Genome-Wide Studies with Multiple Sclerosis
Timasheva, Y.R., Nasibullin, T.R., Tuktarova, I.A., Erdman, V.V., Galiullin, T.R., Zaplakhova, O.V., Bakhtiiarova, K.Z., Mustafina, O.E., Тимашева, Я. Р., Насибуллин, Т.Р., Туктарова, И.А., Эрдман, В.В., Галиуллин, Т.Р., Заплахова, О.В., Бахтиярова, К.З., Мустафина, О.Е. (2021)
РОЛЬ МЕЖГЕННЫХ ВЗАИМОДЕЙСТВИЙ ГЕНОВ НЕЙРОТРОФИЧЕСКОЙ И НЕЙРОМЕДИАТОРНОЙ СИСТЕМЫ В РАЗВИТИИ ПРЕДРАСПОЛОЖЕННОСТИ К ПАРАНОИДНОЙ ШИЗОФРЕНИИ
THE ROLE OF INTERGENIC INTERACTIONS OF NEUROTROPHIC AND NEUROTRANSMITTER SYSTEM GENES IN THE DEVELOPMENT OF SUSCEPTIBILITY TO PARANOID SCHIZOPHRENIA
GAREEVA, A.E., KHUSNUTDINOVA, E.K., ГАРЕЕВА А.Э., ХУСНУТДИНОВА Э. (2020)
) in determining the risk of developing paranoid schizophrenia in ethnic groups of Russians and Tatars.
Investigating the role of osteoprotegerin gene polymorphic variants in osteoporosis
Yalaev, B.I., Tyurin, A.V., Mirgalieva, R.I., Khusnutdinova, E.K., Khusainova, R.I. (2021)
the Volga-Ural region of Russia. Material and Methods - 828 women and 496 men of various ethnic groups
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
FEDOROVA, Y.Y., KARUNAS, A.S., GIMALOVA, G.F., KHUSNUTDINOVA, E.K., SAVELIEVA, O.N, MURZINA, R.R., GATIYATULLIN, R.F., ETKINA, E.I. (2019)
and healthy individuals of Russian, Tatar and Bashkir ethnic origin: rs37973 of the glucocorticoid
IREB2, CHRNA5, CHRNA3, FAM13A & HEDGEHOG INTERACTING PROTEIN GENES POLYMORPHISMS & RISK OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE IN TATAR POPULATION FROM RUSSIA
Korytina, G.F., Akhmadishina, L.Z., Viktorova, E.V., Kochetova, O.V., Viktorova, T.V. (2016)
. Further studies need to be done in other ethnic populations.
HEARING LOSS OF VOLGA-URAL REGION IN RUSSIA
Khusnutdinova, E.K., Dzhemileva, L.U., Lobov, S.L., Kuznetzov, D.U., Nazirova, A.G., Nurgalina, E.M., Barashkov, N.A., Fedorova, S.A. (2017)
is of particular interest, because its ethnic populations mostly belong to the Turkic, Finno-Ugric, and Slavonic

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